Canonical Allele Identifier: PA2827141560
Gene: MCPH1 HGNC NCBI

Linked Data

ClinVar Variation Id: 1350408
ClinVar RCV Id: RCV002039720
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001308974.2:p.Thr434Ser
CA4610543
NM_001322045.2:c.1301C>G
CA370221570
NM_001322045.2:c.1300A>T